Phosphorus-nitrogen compounds: Part 45. Vanillinato-substituted cis-and trans-bisferrocenyldispirocyclotriphosphazenes: Syntheses, spectroscopic and crystallographic characterizations
dc.authorid | Asmafiliz, Nuran/0000-0002-9335-4101 | |
dc.contributor.author | Tumer, Yasemin | |
dc.contributor.author | Asmafiliz, Nuran | |
dc.contributor.author | Arslan, Gonul | |
dc.contributor.author | Kilic, Zeynel | |
dc.contributor.author | Hokelek, Tuncer | |
dc.date.accessioned | 2024-09-29T16:00:26Z | |
dc.date.available | 2024-09-29T16:00:26Z | |
dc.date.issued | 2019 | |
dc.department | Karabük Üniversitesi | en_US |
dc.description.abstract | The nucleophilic replacement reactions of one equimolar amount of the cis- and trans-bisferrocenyldispirocyclotriphosphazenes (1 and 2) with the one equimolar amount of the potassium salt of 4-hydroxy-3-methoxybenzaldehyde (potassium vanillinate) produce mono-vanillinato phosphazenes (3 and 4). When these reactions were carried out with the one equimolar amount of 1 and 2, and two equimolar amounts of potassium vanillinate gave bis-vanillinato ferrocenylphosphazenes (5 and 6). The structures of the new phosphazenes were characterized by FTIR, MS, H-1, C-13 and P-31 NMR spectral data. The solid-state structures of 3, 4, 5 and 6 were clarified by single crystal X-ray diffraction techniques. All the phosphazenes have stereogenic phosphorus atoms. Compound 3 has a pseudo asymmetric center. The absolute configurations of all the compounds were examined using X-ray crystallography. The chiral properties of 3 and 4 were also investigated by P-31 NMR spectroscopy upon the addition of the chiral solvating agent (S)-(+)-2,2,2-trifluoro-1-(9'-anthryl)ethanol, CSA. (C) 2018 Elsevier B.V. All rights reserved. | en_US |
dc.description.sponsorship | Scientific and Technical Research Council of Turkey [216Z182]; Turkish Academy of Sciences (TUBA); Hacettepe University Scientific Research Project Unit [013 D04 602 004] | en_US |
dc.description.sponsorship | The authors acknowledge the Scientific and Technical Research Council of Turkey Grant No. 216Z182. Z.K. thanks the Turkish Academy of Sciences (TUBA) for partial support of this work. T.H. is grateful to Hacettepe University Scientific Research Project Unit (Grant No. 013 D04 602 004). | en_US |
dc.identifier.doi | 10.1016/j.molstruc.2018.12.090 | |
dc.identifier.endpage | 243 | en_US |
dc.identifier.issn | 0022-2860 | |
dc.identifier.issn | 1872-8014 | |
dc.identifier.scopus | 2-s2.0-85059564697 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 235 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.molstruc.2018.12.090 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14619/5131 | |
dc.identifier.volume | 1181 | en_US |
dc.identifier.wos | WOS:000458612300026 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartof | Journal of Molecular Structure | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Ferrocenyldispirophosphazenes | en_US |
dc.subject | Vanillin | en_US |
dc.subject | Crystal structure | en_US |
dc.subject | Spectroscopy | en_US |
dc.subject | Chiral solvating agent | en_US |
dc.title | Phosphorus-nitrogen compounds: Part 45. Vanillinato-substituted cis-and trans-bisferrocenyldispirocyclotriphosphazenes: Syntheses, spectroscopic and crystallographic characterizations | en_US |
dc.type | Article | en_US |